Variant report

Variant	nsv825935
Chromosome Location	chr11:59615227-59626656
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:174)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:174 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:59624956-59625935	K562	blood:	n/a	n/a
2	ATF1	chr11:59625114-59625896	K562	blood:	n/a	n/a
3	ATF3	chr11:59624987-59625918	K562	blood:	n/a	n/a
4	BHLHE40	chr11:59624892-59625750	K562	blood:	n/a	n/a
5	BRCA1	chr11:59624781-59625929	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr11:59625084-59625826	K562	blood:	n/a	n/a
7	CBX3	chr11:59624759-59626039	HCT-116	colon:	n/a	n/a
8	CCNT2	chr11:59625176-59625914	K562	blood:	n/a	n/a
9	CEBPB	chr11:59625170-59625440	K562	blood:	n/a	n/a
10	CEBPB	chr11:59624746-59625949	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:59615132-59615449	K562	blood:	n/a	chr11:59615290-59615301
12	CEBPB	chr11:59624764-59625998	HCT-116	colon:	n/a	n/a
13	CEBPB	chr11:59615165-59615435	HepG2	liver:	n/a	chr11:59615290-59615301
14	CEBPB	chr11:59625123-59625788	K562	blood:	n/a	n/a
15	CEBPD	chr11:59625041-59625936	K562	blood:	n/a	n/a
16	CEBPD	chr11:59625061-59625957	K562	blood:	n/a	n/a
17	CHD2	chr11:59624745-59625895	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr11:59625209-59625763	K562	blood:	n/a	n/a
19	CTCF	chr11:59619740-59619890	GM12873	blood:	n/a	n/a
20	CTCF	chr11:59619864-59619917	K562	blood:	n/a	n/a
21	CTCF	chr11:59619860-59620010	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr11:59619800-59619950	GM12875	blood:	n/a	n/a
23	CTCF	chr11:59619836-59619934	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr11:59619779-59619943	IMR90	lung:	n/a	n/a
25	CTCF	chr11:59619820-59619970	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr11:59625277-59625707	K562	blood:	n/a	n/a
27	CUX1	chr11:59625065-59625994	K562	blood:	n/a	n/a
28	E2F4	chr11:59625561-59625935	MCF10A-Er-Src	breast:	n/a	n/a
29	ELF1	chr11:59625586-59625837	K562	blood:	n/a	chr11:59625728-59625741
30	ELK1	chr11:59625630-59625883	Hela-S3	cervix:	n/a	n/a
31	EP300	chr11:59625174-59625913	K562	blood:	n/a	n/a
32	EP300	chr11:59624755-59626071	Hela-S3	cervix:	n/a	n/a
33	EP300	chr11:59625558-59625789	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr11:59625025-59626024	K562	blood:	n/a	n/a
35	EP300	chr11:59625467-59625887	SK-N-SH_RA	brain:	n/a	n/a
36	FOS	chr11:59624980-59626043	Hela-S3	cervix:	n/a	n/a
37	FOS	chr11:59625021-59625919	K562	blood:	n/a	n/a
38	FOS	chr11:59624925-59625918	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr11:59625053-59625918	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr11:59624900-59625917	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr11:59625264-59625912	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr11:59625038-59625801	HUVEC	blood vessel:	n/a	n/a
43	FOSL1	chr11:59625576-59625881	K562	blood:	n/a	chr11:59625721-59625732
44	FOSL1	chr11:59625052-59625914	K562	blood:	n/a	chr11:59625354-59625365 chr11:59625721-59625732
45	FOSL1	chr11:59625181-59625516	K562	blood:	n/a	chr11:59625354-59625365
46	FOSL1	chr11:59624700-59626149	HCT-116	colon:	n/a	chr11:59625354-59625365 chr11:59625721-59625732 chr11:59626135-59626144
47	FOSL1	chr11:59624764-59626029	HCT-116	colon:	n/a	chr11:59625354-59625365 chr11:59625721-59625732
48	FOSL2	chr11:59625586-59625923	MCF-7	breast:	n/a	n/a
49	GATA1	chr11:59624932-59626000	PBDE	blood:	n/a	n/a
50	GATA2	chr11:59625099-59625865	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:59624274-59624324	RPTEC	kidney:	n/a
2	chr11:59620354-59620404	SK-N-SH	brain:	n/a
3	chr11:59624274-59624324	HEEpiC	esophagus:	n/a
4	chr11:59620354-59620404	HNPCEpiC	eye:	n/a
5	chr11:59624274-59624324	MCF-7	breast:	n/a
6	chr11:59624274-59624324	HAEpiC	amniotic membrane:	n/a
7	chr11:59620354-59620404	GM12878	blood:	n/a
8	chr11:59624274-59624324	NH-A	brain:	n/a
9	chr11:59620354-59620404	MCF10A-Er-Src	breast:	n/a
10	chr11:59624274-59624324	HRPEpiC	eye:	n/a
11	chr11:59624274-59624324	BJ	skin:	n/a
12	chr11:59620354-59620404	NHBE	bronchial:	n/a
13	chr11:59624274-59624324	AG04450	lung:	fetal
14	chr11:59620354-59620404	PFSK-1	brain:	n/a
15	chr11:59624274-59624324	H1-hESC	embryonic stem cell:	embryo
16	chr11:59624274-59624324	Jurkat	blood:	n/a
17	chr11:59620354-59620404	AG10803	skin:	n/a
18	chr11:59620354-59620404	BE2_C	brain:	n/a
19	chr11:59624274-59624324	SK-N-MC	brain:	n/a
20	chr11:59624274-59624324	HEK293	kidney:	embryo
21	chr11:59620354-59620404	HCT-116	colon:	n/a
22	chr11:59624274-59624324	HCPEpiC	choroid plexus:	n/a
23	chr11:59624274-59624324	GM12878	blood:	n/a
24	chr11:59620354-59620404	RPTEC	kidney:	n/a
25	chr11:59624274-59624324	AG04449	skin:	fetal
26	chr11:59620354-59620404	HepG2	liver:	n/a
27	chr11:59624274-59624324	SK-N-SH	brain:	n/a
28	chr11:59624274-59624324	GM06990	blood:	n/a
29	chr11:59624274-59624324	Caco-2	colon:	n/a
30	chr11:59624274-59624324	PFSK-1	brain:	n/a
31	chr11:59624274-59624324	ProgFib	skin:	n/a
32	chr11:59624274-59624324	A549	lung:	n/a
33	chr11:59620354-59620404	Caco-2	colon:	n/a
34	chr11:59620354-59620404	NB4	blood:	n/a
35	chr11:59620354-59620404	AG04449	skin:	fetal
36	chr11:59624274-59624324	LNCaP	prostate:	n/a
37	chr11:59620354-59620404	GM12891	blood:	n/a
38	chr11:59620354-59620404	NT2-D1	testis:	n/a
39	chr11:59624274-59624324	NT2-D1	testis:	n/a
40	chr11:59620354-59620404	SKMC	muscle:	n/a
41	chr11:59620354-59620404	AG09319	gingival:	n/a
42	chr11:59620354-59620404	AG09309	skin:	n/a
43	chr11:59620354-59620404	SK-N-SH_RA	brain:	n/a
44	chr11:59624274-59624324	ECC-1	luminal epithelium:	n/a
45	chr11:59624274-59624324	T-47D	breast:	n/a
46	chr11:59620354-59620404	HRPEpiC	eye:	n/a
47	chr11:59620354-59620404	NH-A	brain:	n/a
48	chr11:59624274-59624324	HIPEpiC	eye:	n/a
49	chr11:59620354-59620404	ProgFib	skin:	n/a
50	chr11:59620354-59620404	ECC-1	luminal epithelium:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:59622551..59626799-chr11:59627538..59631019,5	K562	blood:
2	chr11:59622515..59627357-chr11:59627457..59632233,7	K562	blood:
3	chr11:59625442..59627492-chr11:59632313..59634751,3	MCF-7	breast:
4	chr11:59601837..59604968-chr11:59622137..59625504,3	K562	blood:
5	chr11:59609266..59612061-chr11:59622506..59625749,4	K562	blood:
6	chr11:59618248..59620139-chr11:59644525..59646190,2	K562	blood:
7	chr11:59619737..59621924-chr11:59623514..59625671,2	K562	blood:
8	chr11:59619737..59621924-chr11:59623514..59625671,2	K562	blood:
9	chr11:59614768..59616818-chr11:59620450..59622599,2	K562	blood:
10	chr11:59557627..59559714-chr11:59622962..59625608,2	MCF-7	breast:
11	chr11:59608656..59611754-chr11:59622937..59626902,3	K562	blood:
12	chr11:59619801..59622082-chr11:59633535..59636417,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCN1-1	chr11:59622121-59622240	NONHSAT021548
2	lnc-TCN1-1	chr11:59620676-59620794	NONHSAT021548
3	lnc-TCN1-1	chr11:59620273-59620509	NONHSAT021548

No data

Variant related genes	Relation type
GIF	TF binding region
TCN1	TF binding region
GIF	CpG island
TCN1	CpG island
ENSG00000134827	chromatin interactions
ENSG00000134812	chromatin interactions

Extended variants
information (count: 456 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139826565	chr11:59615246-59615247	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs564418428	chr11:59615262-59615263	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs113204675	chr11:59615309-59615310	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs530599282	chr11:59615317-59615318	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs76238658	chr11:59615345-59615346	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs560992505	chr11:59615350-59615351	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs567293532	chr11:59615379-59615380	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs369137178	chr11:59615418-59615419	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs530025458	chr11:59615467-59615468	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs74704119	chr11:59615470-59615471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs530353326	chr11:59615471-59615472	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs79962666	chr11:59615472-59615473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537875196	chr11:59615481-59615482	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143893470	chr11:59615511-59615512	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs200742078	chr11:59615521-59615522	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577899171	chr11:59615560-59615561	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574566337	chr11:59615573-59615574	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545184910	chr11:59615582-59615583	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs149322057	chr11:59615598-59615599	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs144650948	chr11:59615608-59615609	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs148443866	chr11:59615609-59615610	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527237450	chr11:59615611-59615612	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186250491	chr11:59615631-59615632	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs142622874	chr11:59615634-59615635	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112500280	chr11:59615651-59615652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs188490025	chr11:59615661-59615662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563190013	chr11:59615676-59615677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs181284191	chr11:59615701-59615702	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs552057502	chr11:59615738-59615739	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566687391	chr11:59615745-59615746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185561354	chr11:59615756-59615757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs549042484	chr11:59615780-59615781	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566140978	chr11:59615795-59615796	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs538294009	chr11:59615842-59615843	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs147684643	chr11:59615953-59615954	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs556329670	chr11:59615986-59615987	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs531541976	chr11:59615995-59615996	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs376933382	chr11:59616013-59616014	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs190362024	chr11:59616032-59616033	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs572242018	chr11:59616098-59616099	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs542873855	chr11:59616158-59616159	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs116429579	chr11:59616159-59616160	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs17597065	chr11:59616200-59616201	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs543406358	chr11:59616219-59616220	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs140839103	chr11:59616250-59616251	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs118025661	chr11:59616268-59616269	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs75770337	chr11:59616269-59616270	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs560439356	chr11:59616298-59616299	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs536952665	chr11:59616327-59616328	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs527862052	chr11:59616351-59616352	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59612600-59615400	Enhancers	K562	blood
2	chr11:59613200-59616000	Weak transcription	Fetal Intestine Small	intestine
3	chr11:59613400-59616000	Weak transcription	Fetal Intestine Large	intestine
4	chr11:59614200-59619400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr11:59614600-59616000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr11:59614600-59622000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr11:59614600-59624800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr11:59615000-59615600	Enhancers	Pancreas	Pancrea
9	chr11:59615200-59615400	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr11:59615200-59616200	Weak transcription	Stomach Mucosa	stomach
11	chr11:59615400-59616000	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr11:59615400-59616400	Weak transcription	K562	blood
13	chr11:59615600-59616000	Weak transcription	Pancreas	Pancrea
14	chr11:59616000-59616600	Enhancers	Pancreas	Pancrea
15	chr11:59616000-59617200	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr11:59616000-59617400	Enhancers	Fetal Intestine Large	intestine
17	chr11:59616000-59617400	Enhancers	Fetal Intestine Small	intestine
18	chr11:59616000-59617400	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr11:59616200-59616400	Enhancers	Colonic Mucosa	Colon
20	chr11:59616200-59616400	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr11:59616200-59616600	Enhancers	Duodenum Mucosa	Duodenum
22	chr11:59616200-59616600	Enhancers	Small Intestine	intestine
23	chr11:59616200-59617000	Enhancers	Stomach Mucosa	stomach
24	chr11:59616200-59617200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr11:59616200-59617200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:59616200-59617400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr11:59616400-59616600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
28	chr11:59616400-59617000	Enhancers	K562	blood
29	chr11:59616400-59618200	Weak transcription	Colonic Mucosa	Colon
30	chr11:59616600-59617000	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr11:59616600-59617800	Weak transcription	Pancreas	Pancrea
32	chr11:59617000-59617200	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr11:59617000-59622400	Weak transcription	K562	blood
34	chr11:59617200-59618200	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr11:59617800-59618000	Enhancers	Pancreas	Pancrea
36	chr11:59618000-59624800	Weak transcription	Pancreas	Pancrea
37	chr11:59618200-59618400	Enhancers	Colonic Mucosa	Colon
38	chr11:59618200-59618400	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr11:59619400-59619600	Genic enhancers	Primary neutrophils fromperipheralblood	blood
40	chr11:59619600-59621200	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr11:59621200-59622000	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr11:59622000-59622200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr11:59622000-59622600	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr11:59622200-59623400	Enhancers	Fetal Brain Male	brain
45	chr11:59622200-59624600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr11:59622200-59625000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr11:59622400-59624600	Enhancers	Hela-S3	cervix
48	chr11:59622400-59624800	Enhancers	K562	blood
49	chr11:59622600-59623400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
50	chr11:59623400-59624000	Weak transcription	Primary neutrophils fromperipheralblood	blood

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